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FDA 510(k)

NASO STENT

K-Number: K792556 · 1980-01-16

ApplicantTripedsil, Inc.
Decision Date1980-01-16
Product Code
DecisionSubstantially Equivalent

Device Summary

NASO STENT is the device name listed in this FDA 510(k) record. The listed applicant is Tripedsil, Inc.. It received FDA 510(k) clearance on 1980-01-16 under 510(k) number K792556. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NASO STENT?

NASO STENT is a medical device that received FDA 510(k) clearance on 1980-01-16. The listed applicant is Tripedsil, Inc.. The 510(k) number is K792556.

When did NASO STENT receive FDA 510(k) clearance?

NASO STENT received FDA 510(k) clearance on 1980-01-16, under 510(k) number K792556.

Who is the listed applicant for NASO STENT?

The FDA 510(k) record lists Tripedsil, Inc. as the applicant. This does not by itself establish the device manufacturer.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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